Meckel syndrome and neural tube defects in Kuwait.
作者信息
Teebi A S, al Saleh Q A, Odeh H
出版信息
J Med Genet. 1992 Feb;29(2):140. doi: 10.1136/jmg.29.2.140-a.
Abstract
摘要
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Meckel syndrome and neural tube defects in Kuwait.科威特的梅克尔综合征和神经管缺陷
J Med Genet. 1992 Feb;29(2):140. doi: 10.1136/jmg.29.2.140-a.
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本文引用的文献
1
Phenotypic variation in Meckel syndrome.梅克尔综合征的表型变异
Clin Genet. 1981 Jul;20(1):74-7. doi: 10.1111/j.1399-0004.1981.tb01811.x.
2
The Meckel syndrome: clinicopathological findings in 67 patients.梅克尔综合征：67例患者的临床病理研究结果
Am J Med Genet. 1984 Aug;18(4):671-89. doi: 10.1002/ajmg.1320180414.
3
Meckel syndrome in different populations.
Am J Med Genet. 1984 Aug;18(4):661-9. doi: 10.1002/ajmg.1320180413.
4
Anencephaly: disappearing in Kuwait?无脑儿：在科威特正在消失？
Lancet. 1984 Sep 22;2(8404):701-2. doi: 10.1016/s0140-6736(84)91264-9.
5
High incidence of Meckel's syndrome in Gujarati Indians.古吉拉特印度人群中梅克尔综合征的高发病率。
J Med Genet. 1985 Aug;22(4):301-4. doi: 10.1136/jmg.22.4.301.
6
Nonsyndromal anencephaly: possible autosomal recessive variant.非综合征性无脑畸形：可能的常染色体隐性变异型。
Am J Med Genet. 1986 Jul;24(3):461-4. doi: 10.1002/ajmg.1320240308.
7
Bardet-Biedl and Laurence-Moon syndromes in a mixed Arab population.
Clin Genet. 1988 Feb;33(2):78-82. doi: 10.1111/j.1399-0004.1988.tb03414.x.
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Anencephaly: a vanishing problem in Bedouins?无脑儿：在贝都因人中是一个逐渐消失的问题？
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Phenotypic variability in Meckel-Gruber syndrome.
Clin Genet. 1990 Sep;38(3):176-9. doi: 10.1111/j.1399-0004.1990.tb03568.x.
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